US4037011A - Glass fiber reinforced thermoplastic composition and process for its preparation - Google Patents
Glass fiber reinforced thermoplastic composition and process for its preparation Download PDFInfo
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- US4037011A US4037011A US05/553,962 US55396275A US4037011A US 4037011 A US4037011 A US 4037011A US 55396275 A US55396275 A US 55396275A US 4037011 A US4037011 A US 4037011A
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- thermoplastic resin
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- fiberglass
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
- C08J3/226—Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B15/00—Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00
- B29B15/08—Pretreatment of the material to be shaped, not covered by groups B29B7/00 - B29B13/00 of reinforcements or fillers
- B29B15/10—Coating or impregnating independently of the moulding or shaping step
- B29B15/12—Coating or impregnating independently of the moulding or shaping step of reinforcements of indefinite length
- B29B15/122—Coating or impregnating independently of the moulding or shaping step of reinforcements of indefinite length with a matrix in liquid form, e.g. as melt, solution or latex
- B29B15/125—Coating or impregnating independently of the moulding or shaping step of reinforcements of indefinite length with a matrix in liquid form, e.g. as melt, solution or latex by dipping
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/12—Making granules characterised by structure or composition
- B29B9/14—Making granules characterised by structure or composition fibre-reinforced
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/04—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
- B29C70/06—Fibrous reinforcements only
- B29C70/10—Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres
- B29C70/12—Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres using fibres of short length, e.g. in the form of a mat
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/24—Coatings containing organic materials
- C03C25/26—Macromolecular compounds or prepolymers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249924—Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
- Y10T428/24994—Fiber embedded in or on the surface of a polymeric matrix
- Y10T428/249942—Fibers are aligned substantially parallel
- Y10T428/249946—Glass fiber
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2973—Particular cross section
- Y10T428/2975—Tubular or cellular
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
Definitions
- This invention relates to new compositions of matter comprising fiberglass reinforced thermoplastic resins and more particularly to the art of manufacturing fiberglass reinforced injection molding granule concentrates.
- the invention also provides a new process for manufacture of fiberglass reinforced thermoplastic resin concentrates all as more fully set forth hereinbelow.
- Injection molding glass fiber reinforced thermoplastic resins have, within the past decade, enjoyed a rapid growth because of their superior physical properties as compared to their unreinforced counterparts.
- Brittle resins like homopolymer styrene (crystal or general purpose) have, for example, been improved in kind and have found uses in fields which had hitherto not been open to such resins.
- Reinforcing with glass fibers thus, generally at least doubles tensile strength, improves both low and room temperature impact strengths, increases stiffness, decreases cold flow and coefficient of thermal expansion, increases heat resistance and improves other properties so that such improved properties approach the properties of some metals.
- Fiberglass reinforced injection molding compositions of the type illustrated in the foregoing Table have been described and claimed in U.S. Pat. No. 2,877,501 to R. Bradt, said Patent describing compositions consisting of from 15 to 60 per cent by weight of glass fiber, the remainder being the resin.
- the properties of the fiberglass reinforced thermoplastics prepared from the teachings of U.S. Pat. No. 2,877,501 are the highest properties to be found among fiberglass reinforced thermoplastics.
- a material commonly referred to in the Industry as "short fiberglass” reinforced thermoplastics may be prepared by feeding fiberglass pre-chopped into short, approximately 1/4 inch, lengths together with thermoplastic to the feed pocket of a plastic extruder and co-extruding the mixture of fiberglass and thermoplastic as strands, subsequently cutting these strands into small pellets suitable for injection molding.
- the products produced by this method contain glass fibers dispersed within the granule, but normally the fibers are of an extremely short length, commonly between 0.02 inches to 0.07 inches, despite the fact that much longer glass fibers are fed to the extruder.
- the fiber length reduction is caused by the extensive grinding action which takes place among the hard thermoplastic pellets and fiberglass as the mixture is compressed in the feed screw of the extruder.
- the ultimate physical properties of these so-called “short glass” reinforced thermoplastics are not equivalent to those known as the "long glass” reinforced thermoplastics. This non-equivalence is illustrated by a comparison of the physical properties shown in the following Table.
- short glass reinforced nylon yields maximum tensile strengths of only 24,000 psi while long glass reinforced nylon yields tensile strengths of 30,000 psi.
- Izod impact strengths of the short glass products are considerable below those of the long glass counterparts.
- short glass nylon yields an Izod impact strength of only 1.4 ft. lb./in.
- long glass reinforced nylon yields an Izod impact strength of 3.4 ft. lbs./in.
- the discrepancy between long and short glass reinforced polystyrenes is even more dramatic.
- Short glass polystyrenes have an impact strength of only 0.5 ft. lb./in. while long glass reinforced polystyrenes have an impact strength of 2.5 ft. lb./in.
- One method relates the feeding of pre-chopped fiberglass and non-reinforced thermoplastic in separate streams to the hopper of the screw injection molding machine while the second method concerns the chopping of continuous strand fiberglass roving directly above the injection molding machine hopper and the freshly chopped glass is mixed in the hopper with non-reinforced thermoplastic resin.
- both of these systems fail to adequately disperse the fiberglass within the plastic resin and often lead to the formation of clumps of fiberglass and resin-rich areas in the molded part. Formation of clumps and/or resin-rich areas leads to erratic and non-uniform physical properties throughout the molded piece. Fiberglass clumps also have a tendency to collect on the surface of the molded articles interferring with subsequent operations such as painting, vacuum metalizing, or plating. Further in operation involving the second method described above chopping of continuous strand fiberglass roving produces large amounts of extremely fine fiberglass which tends to float through the air constituting a major housekeeping problem and health hazard.
- binder resins are put on fiberglass by the fiberglass manufacturer to facilitate the handling of the continuous fiberglass roving and its subsequent chopping into short lengths.
- the choice of these binder resins is made to facilitate handling and often the resins are incompatible with a thermoplastic into which the fiberglass is subsequently incorporated. Such incompatibility leads to poor physical properties as a result of the non-wetting of the fiberglass surface by the thermoplastic resin.
- Fiberglass manufacturers apply one to two per cent of binder resin to the surface of the fiberglass as common practice, although the literature mentions higher percentages.
- the fiberglass reinforced thermoplastic materials which are available commercially as a result of the prior art consist of the superior physical property materials prepared by employing long glass fibers, the short glass fiber materials prepared by extrusion compounding, and those products prepared by the direct mixing of fiberglass and thermoplastic in a screw injection molding machine.
- the direct mix system provides the most competitive economics but has unacceptable disadvantages.
- the teachings of the Bradt Patent provide the best possible physical properties but do not permit manufacture of a product economically competitive with the direct mix system.
- thermoplastic resin which can be mixed at an injection molding machine hopper with non-reinforced thermoplastic with resultant economics competitive with the direct mixing of bare fiberglass and thermoplastic resin.
- thermoplastic resin of the same type as and chosen to be compatible with the non-reinforced thermoplastic resin with which it is ultimately intended to be mixed in the injection molding machine.
- a rigid fiberglass reinforced thermoplastic injection molding granule comprising a thermoplastic resin incorporating a multiplicity of glass filaments which are substantially surrounded and bonded by said thermoplastic resin, said granule being resistant to splitting and having glass filaments extending predominantly throughout the length of the granule and in substantially parallel direction thereto, the amount by weight of said glass filaments ranging from about 70% to about 90%, the remainder consisting essentially of resin, the length of said granule being at least 1/8 of an inch.
- This invention also provides a method for preparing the injection molding concentrate as set forth above, said process comprising the steps of, (a) continuously passing a length of glass filaments (roving or strand) through a reservoir of a thermoplastic resin and impregnating said filaments with from about 10 to 30 per cent by weight of said resin, (b) passing the thermoplastic resin impregnated glass filaments to a cutting zone wherein said impregnated filaments are cut to granules at least 1/8 inch long, said cutting occurring while the strand is maintained under controlled temperature conditions.
- long fiberglass means glass filaments greater than 1/8 of an inch long and extending substantially the full length of the granule, whereas “short” fiberglass means glass filaments of less than 1/8 inch in length;
- impregnating refers to the permeation of fiberglass strand by a thermoplastic resin in such a manner that under the optimum condition each individual glass filament is coated and substantially wetted by the thermoplastic resin;
- FIG. I is a block flow diagram showing apparatus suitable for use in practicing one form of the process of this invention.
- FIG. II is a diagramatic plan view illustrating another form of apparatus suitable for use in practicing another form of the process of this invention.
- glass strands or rovings 10 are fed from suitable creels 11, through a bath shown generally at 12 which bath can be in the form of a water emulsion or solution of the thermoplastic resin or a solution of the thermoplastic resin is an appropriate solvent which impregnates the strand or roving.
- the strand is next passed through an oven 13 in which the water of the emulsion, or the solvent of the solution, is driven off and the resin fused.
- glass strands or rovings 20 are fed from a suitable creel (not shown) and are passed through a trough 21 containing a suitable resin emulsion or solution, if a preimpregnation of the strands is necessary. As they pass through the trough, the strands or rovings are impregnated with the resin. Leaving the trough 21, the impregnated strands or rovings pass through an oven 22 in which any volatiles are driven off and the resin fused. Emerging from the oven 22, the strands or rovings pass into a chamber 23, hereinafter referred to as a reservoir, containing a supply of molten thermoplastic resin.
- the reservoir 23 contains a gathering die 24 which gathers the strands into a single bundle 25 which emerges from the reservoir through an orifice in alignment with the gathering die 24.
- the bundle 25 passes between power driven feed rolls 27 which serve to draw the strands or rovings through the apparatus. After leaving the rolls 27, the bundle passes into association with a shear 28 which cuts it into short lengths to form the desired pellets or granules.
- impregnated strand may be passed near a series of heaters, shown generally at 29, wherein the temperature of the strand is raised to an appropriate temperature wherein it will be ready for pelletizing in unit 28.
- FIG. II refers to general process steps a more complete and detailed description of the apparatus can be had by reference to U.S. Pat. No. 3,042,570, the disclosure of which is incorporated herein by reference. It should be mentioned here that although in neither U.S. Pat. Nos. 3,119,718 or 3,042,570 is there a positive heating step shown for the impregnated strand prior to pelletizing, in order to have the strand in a condition suitable for pelletizing such a heating step can be necessary and as such can be readily provided as shown generally in FIG. I by the use of lamps such as infrared lamps or by any other suitable heating source.
- lamps such as infrared lamps or by any other suitable heating source.
- each strand or roving can comprise about eight to 120 "ends.” Each "end” is formed of approximately 200 individual glass filaments. Where good contact between the glass filaments and the resin is of importance, it may be desirable to reduce the number of "ends" in each strand or roving.
- the apparatus used in the application of the respective resins may take different forms depending upon such factors as manufacturing convenience, the types of resins applied, and the necessary characteristics of the final product.
- the invention in its broader aspects is therefore not limited to any specific type of impregnating or coating apparatus. While the apparatus employing impregnators of the respective types above described has wide application, the resins might be applied by passing the strands or rovings through liquid dispersions or might be applied by melt-coaters. In some cases, it may be convenient to apply the resin through the use of a transfer or kiss roll running partially immersed in a resin bath.
- the liquid impregnating and coating material may be in any suitable form such as an emulsion, a solution, a prepolymer, or even a monomer.
- the bath may contain an appropriate polymerization catalyst and may be brought to the desired viscosity by incorporation of finely divided polymer. The viscosity of a bath will influence the amount of bath material picked up by a strand or roving passing through it.
- a process for preparing a concentrate for use in injection molding compositions said concentrate also constituting a new composition of matter.
- the process for preparing the concentrate embodies certain critical steps which if not practiced will lead to failure.
- the art or process sought to be patented herein relates to the manufacture of a pellet which can be added with pellets of unreinforced thermoplastic resin to the feed hopper of an injection molding machine to obtain an injection molded article having vastly superior properties as compared to the unreinforced article.
- thermoplastic resin to the glass fiber is a continuous method, wherein roving strands are passed through a reservoir containing an emulsion of polystyrene, for example.
- the strands are opened up by any suitable means prior to introduction into the reservoir of thermoplastic resin, or while immersed in the resin reservoir, and the amount of resin picked up by the strand is controlled by any one of the following:
- thermoplastic in the emulsion or solution b. concentration of thermoplastic in the emulsion or solution
- thermoplastic emulsion a viscosity of thermoplastic emulsion, solution or melt
- the degree to which the excess resin is wipped off by suitable mechanisms such as by passing the strand through a restricting orifice.
- the amount of resin picked up by the roving can be critically controlled by manipulation of any of the above variables.
- thermoplastic resin reservoir After passage of the roving through the thermoplastic resin reservoir, it can then be passed through an oven maintained at 400° to 700° F. to remove water and/or other volatiles and to fuse the resin.
- the specific temperatures employed in the oven will depend upon the resins employed and the means of putting them on to the fiberglass roving.
- emulsions of the thermoplastic resin have been used to impregnate the fiberglass roving, considerable heat must be used to drive off the water present in the emulsion.
- certain thermoplastic resins and particularly when these resins have been applied from solution it may be desirable to accomplish the foregoing in two distinct steps.
- thermoplastic resin solution After passage of the roving through the thermoplastic resin solution, it can then be passed through an oven maintained at a lower temperature to remove the solvent without danger of fire or explosion from the solvent vapors. Subsequently, the strand is passed through a second oven or a higher temperature zone in the same oven maintained at 400° to 700° F. in order to carry out this step of fusing the thermoplastic resin to the fiberglass roving.
- a second oven or a higher temperature zone in the same oven maintained at 400° to 700° F. in order to carry out this step of fusing the thermoplastic resin to the fiberglass roving.
- the strands or rovings can be taken from the melt impregnating zone to a cooling zone and cooled sufficiently so that the strands may be handled.
- the strands or rovings can be taken from the heating zone (emulsion or solution impregnation) and if required further heating can be applied to the strand (by any of the convenient heating means previously described) in order to bring the strands to proper cutting temperatures.
- the strands of rovings of thermoplastic impregnated fiberglass must be cut or pelletized above a certain minimum temperature if a suitable yield of acceptable pellets is to be obtained.
- the minimum cutting temperature for each thermoplastic impregnated fiberglass strand is not related to the amorphous or crystalline character of the thermoplastic on the strand but is routinely determined in the practice of the process. In general, it has been found that the minimum cutting temperature is 80° F. When producing short length pellets, from 1/8 inch to 1/4 inch long, where shattering during pelletizing is a problem, the minimum cutting temperatures must be, in general, higher than those required to cut longer pellets, say 1/2 inch long.
- the temperature of the strand must not be so high as to cause cut pellets to stick, that is, the resin must not be heated to the sticky stage. In addition, the temperature of the strand must not be so high as to cause the strand to stick to the pull rolls. When the strand is not up to the proper temperature, then acceptable pelletizing thereof does not occur and the product is a mass of shattered fiberglass and resin. It is a further critical feature of the injection molding granule concentrate herein described that the size or length of the granule must be at least 1/8 inch to 1/4 inch long and preferably 1/2 of an inch long before an acceptable pellet can be obtained.
- the length of the pellet is less than 1/8 to 1/4 of an inch long, then the product shatters badly during pelletizing and it is not possible to produce an acceptable injection molding composition. It is further preferred in accordance with this invention that the diameter of the granule be at least about one sixteenth of an inch. Examples will be presented hereinafter to illustrate some of the points above.
- the injection molding concentrate granules of this invention must possess certain minimum physical properties in order to be useful as concentrates for injection molding. These compositions must possess stiffness, that is, the impregnated strands and also be resulting pellets must be relatively stiff in order to be handled in the process and also must possess a certain "splitting"resistance essential to the pelletizing operation and subsequently handling of the pellets. These characteristics will be further defined and illustrated by example hereinafter.
- the injection molding concentrate granule of this invention must possess a certain minimum pellet integrity so that they may be handled by the many varied techniques conventionally employed in the Plastics Industry, such as screw auger conveying, feeding from vibratory type hoppers, bin storage and withdrawal, drum tumbling and blending, ribbon blending, double-cone blending, or other handling methods where the pellets are subjected to impact or attrition forces.
- the concentrate granules can be suitably blended with unreinforced resins suitable for extrusion, blow molding, transfer and compression molding techniques.
- a series of 60 end glass roving strands were passed through a polystyrene emulsion as set forth in FIG. I.
- the glass roving after immersion in the emulsion was wiped and dried to leave 20 percent resin with the remaining 80 percent by weight being glass fibers.
- the wet roving was passed through an oven at 500° to 600° F. to first drive off the water from the emulsion and then to fuse the resin around the glass roving.
- the resin coated strand was maintained at a temperature of about 150° F. by use of infrared heaters and at this temperature was successfully chopped into pellets approximately 1/2 inch long.
- the glass fiber concentrated injection molding granules were thereafter blended with unreinforced polystyrene pellets to provide a molding composition containing a range of useful glass contents.
- Table III shows examples of physical properties of such blends containing 0, 20 and 35% glass reinforcement.
- Table III illustrates the ultimate utility of the concentrates of this invention.
- a similar product was prepared from a styreneacrylonitrile latex under similar conditions.
- a polypropylene resin was melted in an extruder and used to impregnate directly a glass roving as illustrated in FIG. II to obtain a product containing about 75 percent glass.
- the strands were successfully cut into pellets of about 3/8 of an inch in length while being maintained at a temperature of about 180° F.
- the pellets were thereafter blended with non-reinforced polypropylene to a 20% total glass content. The following physical properties wee obtained by molding this blend.
- a series of 60 end glass roving strands were passed through a commercial polyurethane emulsion as set forth in FIG. I.
- the glass roving after emergence from the emulsion was wiped and dried to leave 20% resin with the remaining 80% by weight being glass fibers.
- the wet roving was passed through an oven at about 500° F. to first drive off the water from the emulsion and then fuse the polyurethane resin around the glass filaments.
- the resin coated strand was maintained at a temperature of about 150° F. and at this temperature was successfully chopped into pellets of approximately 1/2 inch long.
- the glass fiber concentrated injection molding granules were thereafter blended with unreinforced resin and molded into test specimens. Similar improved properties were observed.
- An emulsion of high density polyethylene powder in water was prepared separately.
- a series of 60 end glass roving strands were then passed through this emulsion as set forth in FIG. I.
- the glass roving after immersion in the emulsion was wiped and dried to leave 20% resin with the remaining 80% by weight being glass fibers.
- the wet roving was passed through an oven at 550° F. to first drive off the water from the emulsion and then to fuse the polyethylene resin around the glass filaments.
- the polyethylene resin impregnated strand was maintained at a temperature of about 150° F. and at this temperature was successfully chopped into pellets approximately 1/2 inch long.
- the glass fiber concentrated injection molding granules were thereafter blended with unreinforced polyethylene pellets to provide a molding composition containing 20% glass. This molding composition was injection molded into test specimens which exhibited the following properties.
- a solution of general purpose polystyrene resin in toluene as a solvent was prepared to contain approximately 5% polystyrene.
- a series of 60 end glass roving strands were then passed through this solution as set forth in FIG. I.
- the glass roving after immersion in the solution was wiped and dried to leave 25% resin with the remaining 75% by weight being glass fibers.
- the wet roving was passed through an oven at 400° F. to first drive off the toluene from the solution and then to fuse the polystyrene resin around the glass filaments.
- the polystyrene resin impregnated strand was maintained at a temperature of about 150° F. and at this temperature was successfully chopped into pellets approximately 1/2 inch long.
- the glass fiber concentrated injection molding granules were thereafter blended with unreinforced polystyrene pellets to provide a molding composition containing 20% glass.
- This molding composition was injection molded into test specimens which exhibited properties similar to those shown in Table III for 20% fiberglass.
- the concentrate pellet must be cut at a certain elevated temperature which will vary from resin to resin but which elevated temperature is nevertheless required in order to obtain the results of this invention.
- a suitable strand temperature for cutting or pelletizing is about 80° F. to about 170° F., preferrably 100° to about 160° F.
- the same temperature range applies to concentrates prepared from styrene-acrylonitrile copolymers (SAN).
- SAN styrene-acrylonitrile copolymers
- the pelletizing operation can be successfully performed and yields an acceptable minimum number of split and shattered pellets.
- pelletizing temperatures should be above 80° F., preferably above 90° F. but below a temperature at which the cut pellets would tend to agglomerate due to sticking.
- Other suitable temperatures are:
- the physical properties of the concentrates themselves in strand or pellet form would not normally be determined because the principle end use for these concentrates is to blend with non-reinforced resins, to further characterize the nature of these concentrates, the following properties have been determined.
- Table VI the Izod impact strength of a single strand of 60 end fiberglass impregnated with polystyrene resin was determined following the general procedure and equipment specified in ASTM Test D-256-56. Obviously the sample holder was modified to support the single strand sample. As the glass content of the strand was varied, the Izod impact strength rose rapidly and then decreased as 100% glass was approached.
- splitting resistance of a pellet is preferably about 100 pounds per square inch. Splitting resistance of a pellet was determined by measuring the force required to push an ordinary Embroidery No 1 sewing needle through a diameter of the pellet at a rate of 0.1 inches per minute. The force was measured on a standard Instron Tester and the value was divided by the cross sectional area of the pellet to put the values on the same basis. Polystyrene impregnated pellets were used for all of this work.
- thermoplastic resins include polystyrene, the acrylic resins, acrylonitrile-butadiene-styrene (ABS) resins, polyvinyl chloride resins, polyformaldehyde resins, polysulfone resins, polyphenylene oxide resins, polyamide resins such as nylon, polyester resins, polyolefin resins, polycarbonate resins, and many others.
- the rovings or glass strands used in this invention can be sized with many commercially available sizes such as polyesters, polyvinyl-acetates and/or coupling agents of the silane or chrome-complex type.
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Abstract
Description
TABLE I __________________________________________________________________________ 40% fiber- 35% fiber- 40% fiber- glass rein- glass rein- Unreinforced glass rein- ASTM Unreinforced forced Unreinforced forced Polyethylene forced Property Unit Test Nylon 6 , 6 nylon 6 , 6 Polystyrene Polystyrene (high density) Polyethylene __________________________________________________________________________ Tensile Strength PSI D638-61T 11,800 30,000 7,500 15,000 4,200 11,000 Elongation % D638-61T 60 2.2 3.0 1.2 800 3.5 Tensile Modulus PSI×10.sup.5 D638-61T 4.5 20 4.6 19 1.4 9.0 Izod Impact Ft.lbs/in. D256-56 1.0 3.4 0.5 2.2 2.0 4.0 Deflection Temp. °F. D648-56 150 500 180 220 175 260 Under Load at (at 66 psi) 264 psi Linear Coefficient In/in ° F D696-44 4.5×10.sup..sup.-5 1.4×10.sup..sup.-5 4×10.sup..sup.-5 1.8×10.sup..sup.-5 6×10.sup..sup.-5 1.7×10.sup.. sup.-5 of Termal Expansion __________________________________________________________________________
TABLE II __________________________________________________________________________ Long Glass Short Glass Long Glass Short Glass ASTM Nylon 6-6 Nylon 6-6 Polystyrene Polystyrene Property Test 40% glass 40% glass 30% glass 30% glass __________________________________________________________________________ Tensile strength D638-61T 30,000 24,000 14,000 11,000 at 73° F. psi Flexural Modulus D790-63 18.0 15.0 12.0 10.0 at 73° F. psi × 10.sup.5 Izod Impact D256-56 3.4 1.4 2.5 0.5 73° F. Ft.lb./In. Deflection Temp. D648-56 500 480 220 210 under load at 264 psi ° F. __________________________________________________________________________
TABLE III __________________________________________________________________________ Property ASTMO% Glass 20% Glass 35% Glass __________________________________________________________________________ Tensile strength psi D638-61T 8,100 12,000 14,000 Elongation, % D638-61T 2.2 2.0 2.0 Tensile Modulus, psi D638-61T 460,000 840,000 1,200,000 Notched Izod Impact D256-56 0.3 1.5 2.5 Strength, ft.lb./in. Deflection Temp. ° F. D648-56 199 218 222 at 264 psi __________________________________________________________________________
TABLE IV ______________________________________ ASTM Test Tensile Strength, psi D638-61T 6,000 Flexural Strength, psi D790-63 7,000 Izod Impact, ft.lb/in. D256-56 2.3 Deflection Temp. at 264 D648-36 280 psi, ° F ______________________________________
TABLE V ______________________________________ ASTM Test Tensile Strength, psi D638-61T 6,500 Flexural Strength, psi D790-63 8,000 Izod Impact Ft. lbs/in. D256-56 2.0 Deflection Temp. at 264 D648-56 260 psi, ° F. ______________________________________
TABLE VI ______________________________________ Izod Impact % Glass Ft.Lbs./in. ______________________________________ 0 2.4 30 20 80 13 90 4 100 0 ______________________________________
TABLE VII ______________________________________ Splitting Resistance % Glass lb./in. ______________________________________ 0 2,700 30 1,600 80 900 90 180 100 0 ______________________________________
Claims (13)
Priority Applications (1)
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US05/553,962 US4037011A (en) | 1972-02-15 | 1975-02-28 | Glass fiber reinforced thermoplastic composition and process for its preparation |
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US22641872A | 1972-02-15 | 1972-02-15 | |
US05/553,962 US4037011A (en) | 1972-02-15 | 1975-02-28 | Glass fiber reinforced thermoplastic composition and process for its preparation |
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US22641872A Continuation | 1972-02-15 | 1972-02-15 |
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US4037011A true US4037011A (en) | 1977-07-19 |
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US05/553,962 Expired - Lifetime US4037011A (en) | 1972-02-15 | 1975-02-28 | Glass fiber reinforced thermoplastic composition and process for its preparation |
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US4157326A (en) * | 1977-11-28 | 1979-06-05 | Monsanto Company | Preparation of glass concentrate capsules for reinforcement of thermoplastics |
US4169186A (en) * | 1978-04-17 | 1979-09-25 | Asahi-Dow Limited | Molding material structure |
US4335167A (en) * | 1980-06-02 | 1982-06-15 | Edison International, Inc. | Brake fluid reservoir comprising polymethylpentene and 10-20% glass fibers |
EP0056703A1 (en) * | 1981-01-21 | 1982-07-28 | Imperial Chemical Industries Plc | Fibre-reinforced compositions and methods for producing such compositions |
FR2519180A1 (en) * | 1981-12-30 | 1983-07-01 | Bekaert Sa Nv | PLASTIC ARTICLE CONTAINING CONDUCTIVE FIBERS IN ELECTRICITY |
EP0208873A2 (en) * | 1985-06-13 | 1987-01-21 | American Cyanamid Company | Elongated molding granules and injection-molding process employing them |
US4664971A (en) * | 1981-12-30 | 1987-05-12 | N.V. Bekaert S.A. | Plastic article containing electrically conductive fibers |
US4808481A (en) * | 1986-10-31 | 1989-02-28 | American Cyanamid Company | Injection molding granules comprising copper coated fibers |
US4818615A (en) * | 1986-06-02 | 1989-04-04 | American Cyanamid Company | Elongated molding granules and injection-molding process employing them |
AU583374B2 (en) * | 1981-01-21 | 1989-04-27 | Imperial Chemical Industries Plc | Fibre-reinforced pellet |
US5019450A (en) * | 1981-01-21 | 1991-05-28 | Imperial Chemical Industries Plc | Fiber reinforced compositions and method of producing such compositions |
EP0440970A2 (en) * | 1990-01-23 | 1991-08-14 | Cytec Technology Corp. | Molding granules, their manufacture and their use in the production of molded particles |
US5091255A (en) * | 1990-01-23 | 1992-02-25 | American Cyanamid Company | Molding granules, their manufacture and their use in the production of molded articles |
US5132342A (en) * | 1991-04-16 | 1992-07-21 | E. I. Du Pont De Nemours And Company | Nonsegregating blends of glass fibers and polymer pellets |
US5213889A (en) * | 1981-01-21 | 1993-05-25 | Imperial Chemical Industries Plc | Fibre-reinforced compositions and methods for producing such compositions |
US5236781A (en) * | 1990-01-31 | 1993-08-17 | Stamicarbon B.V. | Plastic granulate containing non-dispersed reinforcing fibre bundles |
US5430076A (en) * | 1993-01-26 | 1995-07-04 | Asahi Fiber Glass Company Limited | Glass fiber strand for reinforcing a thermoplastic resin and process for preparing a fiber-reinforced resin product |
US5532054A (en) * | 1988-09-20 | 1996-07-02 | Mitsui Toatsu Chemicals, Inc. | Molding material |
US5700556A (en) * | 1993-02-19 | 1997-12-23 | Hoechst Aktiengesellschaft | Granules of fiber-reinforced thermoplastic |
EP0822056A2 (en) * | 1996-07-30 | 1998-02-04 | KABUSHIKI KAISHA KOBE SEIKO SHO also known as Kobe Steel Ltd. | Fibre reinforced compositons and methods for their production |
US5891560A (en) * | 1997-07-02 | 1999-04-06 | The Dow Chemical Company | Fiber-reinforced composite and method of making same |
US5989710A (en) * | 1988-10-21 | 1999-11-23 | Toyo Boseki Kabushiki Kaisha | Molding material for thermoplastic composites |
US6143410A (en) * | 1994-11-02 | 2000-11-07 | Materials Research Innovations Corporation | Folded fiber filled molding material |
US6162536A (en) * | 1999-02-10 | 2000-12-19 | Montsinger; Lawrence V. | Conductive long fiber polyvinyl chloride composites |
US6171492B1 (en) | 1999-02-04 | 2001-01-09 | Purolator Products Company | Filter for liquid fuel |
WO2001010618A1 (en) * | 1999-08-04 | 2001-02-15 | Neopreg Ag | Fiber-reinforced synthetic material granulates |
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US6365090B1 (en) | 1999-07-16 | 2002-04-02 | Owens Corning Fiberglas Technology, Inc. | System for preparing polymer encapsulated glass fiber pellets |
US6872343B2 (en) * | 2000-01-13 | 2005-03-29 | Fulcrum Composites, Inc. | Process for in-line forming of pultruded composites |
WO2006095101A1 (en) | 2005-03-09 | 2006-09-14 | Saint-Gobain Vetrotex France S.A. | Concentrated reinforcing bars and method for making same |
WO2007008632A2 (en) | 2005-07-07 | 2007-01-18 | Dow Global Technologies Inc. | Long fiber-reinforced thermoplastic concentrate and method for its preparation |
US20070104752A1 (en) * | 2003-12-10 | 2007-05-10 | Lee Jeffrey A | Aneurysm embolization material and device |
US20080109057A1 (en) * | 2003-12-10 | 2008-05-08 | Calabria Marie F | Multiple point detacher system |
US20090227976A1 (en) * | 2008-03-05 | 2009-09-10 | Calabria Marie F | Multiple biocompatible polymeric strand aneurysm embolization system and method |
EP2543691A3 (en) * | 2007-09-28 | 2013-10-30 | Dow Global Technologies LLC | Method to make a long fiber concentrate with a dispersion of higher crystallinity olefin |
WO2016091686A1 (en) | 2014-12-08 | 2016-06-16 | Sabic Global Technologies B.V. | Process for the manufacture of glass fibre reinforced pellets |
US20160332345A1 (en) * | 2013-07-03 | 2016-11-17 | Hilti Aktiengesellschaft | Method and injection molding system for producing intumescent reaction plastic molded parts and reaction plastic molded part |
US20190284352A1 (en) * | 2013-03-07 | 2019-09-19 | Johns Manville | Fiber reinforced composites made with coupling-activator treated fibers and activator containing reactive resin |
US11358347B2 (en) * | 2019-02-21 | 2022-06-14 | Johns Manville | Manufacturing fiber-reinforced thermoplastic concentrates |
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Cited By (57)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4157326A (en) * | 1977-11-28 | 1979-06-05 | Monsanto Company | Preparation of glass concentrate capsules for reinforcement of thermoplastics |
US4169186A (en) * | 1978-04-17 | 1979-09-25 | Asahi-Dow Limited | Molding material structure |
US4335167A (en) * | 1980-06-02 | 1982-06-15 | Edison International, Inc. | Brake fluid reservoir comprising polymethylpentene and 10-20% glass fibers |
AU583374B2 (en) * | 1981-01-21 | 1989-04-27 | Imperial Chemical Industries Plc | Fibre-reinforced pellet |
EP0056703A1 (en) * | 1981-01-21 | 1982-07-28 | Imperial Chemical Industries Plc | Fibre-reinforced compositions and methods for producing such compositions |
US5213889A (en) * | 1981-01-21 | 1993-05-25 | Imperial Chemical Industries Plc | Fibre-reinforced compositions and methods for producing such compositions |
US5019450A (en) * | 1981-01-21 | 1991-05-28 | Imperial Chemical Industries Plc | Fiber reinforced compositions and method of producing such compositions |
US5397608A (en) * | 1981-12-30 | 1995-03-14 | Soens; Lode J. | Plastic article containing electrically conductive fibers |
US4664971A (en) * | 1981-12-30 | 1987-05-12 | N.V. Bekaert S.A. | Plastic article containing electrically conductive fibers |
FR2519180A1 (en) * | 1981-12-30 | 1983-07-01 | Bekaert Sa Nv | PLASTIC ARTICLE CONTAINING CONDUCTIVE FIBERS IN ELECTRICITY |
EP0208873A2 (en) * | 1985-06-13 | 1987-01-21 | American Cyanamid Company | Elongated molding granules and injection-molding process employing them |
EP0208873A3 (en) * | 1985-06-13 | 1988-03-02 | American Cyanamid Company | Elongated molding granules and injection-molding process employing them |
US4818615A (en) * | 1986-06-02 | 1989-04-04 | American Cyanamid Company | Elongated molding granules and injection-molding process employing them |
US4808481A (en) * | 1986-10-31 | 1989-02-28 | American Cyanamid Company | Injection molding granules comprising copper coated fibers |
US5532054A (en) * | 1988-09-20 | 1996-07-02 | Mitsui Toatsu Chemicals, Inc. | Molding material |
US5989710A (en) * | 1988-10-21 | 1999-11-23 | Toyo Boseki Kabushiki Kaisha | Molding material for thermoplastic composites |
US5091255A (en) * | 1990-01-23 | 1992-02-25 | American Cyanamid Company | Molding granules, their manufacture and their use in the production of molded articles |
EP0440970A3 (en) * | 1990-01-23 | 1992-01-15 | American Cyanamid Company | Molding granules, their manufacture and their use in the production of molded particles |
EP0440970A2 (en) * | 1990-01-23 | 1991-08-14 | Cytec Technology Corp. | Molding granules, their manufacture and their use in the production of molded particles |
US5236781A (en) * | 1990-01-31 | 1993-08-17 | Stamicarbon B.V. | Plastic granulate containing non-dispersed reinforcing fibre bundles |
US5132342A (en) * | 1991-04-16 | 1992-07-21 | E. I. Du Pont De Nemours And Company | Nonsegregating blends of glass fibers and polymer pellets |
US5430076A (en) * | 1993-01-26 | 1995-07-04 | Asahi Fiber Glass Company Limited | Glass fiber strand for reinforcing a thermoplastic resin and process for preparing a fiber-reinforced resin product |
US5700556A (en) * | 1993-02-19 | 1997-12-23 | Hoechst Aktiengesellschaft | Granules of fiber-reinforced thermoplastic |
US6143410A (en) * | 1994-11-02 | 2000-11-07 | Materials Research Innovations Corporation | Folded fiber filled molding material |
EP0822056A2 (en) * | 1996-07-30 | 1998-02-04 | KABUSHIKI KAISHA KOBE SEIKO SHO also known as Kobe Steel Ltd. | Fibre reinforced compositons and methods for their production |
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US5935508A (en) * | 1996-07-30 | 1999-08-10 | Kabushiki Kaisha Kobe Seiko Sho | Fibre-reinforced compositions and methods for their production |
US6165604A (en) * | 1997-07-02 | 2000-12-26 | The Dow Chemical Company | Fiber-reinforced composite and method of making same |
US5891560A (en) * | 1997-07-02 | 1999-04-06 | The Dow Chemical Company | Fiber-reinforced composite and method of making same |
US6171492B1 (en) | 1999-02-04 | 2001-01-09 | Purolator Products Company | Filter for liquid fuel |
US6162536A (en) * | 1999-02-10 | 2000-12-19 | Montsinger; Lawrence V. | Conductive long fiber polyvinyl chloride composites |
US6365090B1 (en) | 1999-07-16 | 2002-04-02 | Owens Corning Fiberglas Technology, Inc. | System for preparing polymer encapsulated glass fiber pellets |
US6659756B2 (en) | 1999-07-16 | 2003-12-09 | Owens Corning Fiberglas Technology, Inc. | System for preparing polymer encapsulated glass fiber pellets |
WO2001010618A1 (en) * | 1999-08-04 | 2001-02-15 | Neopreg Ag | Fiber-reinforced synthetic material granulates |
WO2001028765A1 (en) * | 1999-10-15 | 2001-04-26 | Wabash Technology Corporation | Roof sheet for a trailer |
US6872343B2 (en) * | 2000-01-13 | 2005-03-29 | Fulcrum Composites, Inc. | Process for in-line forming of pultruded composites |
US20070104752A1 (en) * | 2003-12-10 | 2007-05-10 | Lee Jeffrey A | Aneurysm embolization material and device |
US20080109057A1 (en) * | 2003-12-10 | 2008-05-08 | Calabria Marie F | Multiple point detacher system |
US20080171200A1 (en) * | 2005-03-09 | 2008-07-17 | Philippe Pardo | Concentrated Reinforcing Bars And Method For Making Same |
FR2882958A1 (en) * | 2005-03-09 | 2006-09-15 | Saint Gobain Vetrotex | CONCENTRATED REINFORCING STICKS AND THEIR MANUFACTURE |
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US20090227976A1 (en) * | 2008-03-05 | 2009-09-10 | Calabria Marie F | Multiple biocompatible polymeric strand aneurysm embolization system and method |
US20190284352A1 (en) * | 2013-03-07 | 2019-09-19 | Johns Manville | Fiber reinforced composites made with coupling-activator treated fibers and activator containing reactive resin |
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